Viper 286760210
by Depuy Spine, Inc. EUDAMEDGUDID
Active
Ref 286760210Model Viper Reusable Instruments for Insertion and Extraction
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0705034a001365W | Date24 Dec 2025 | StatusActive |
| United States | GUDID listing GUDID | Number10705034214924 | Date31 Dec 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- VIPER2 System EUDAMEDViper GUDID
- Generic Name
- Orthopaedic implant impactor, reusable
- Model / Ref / Catalog
- 286760210, Viper Reusable Instruments for Insertion and Extraction
- Primary DI / UDI-DI
- 10705034214924
- Basic UDI-DI
- 0705034a001365W
- Direct Marketing DI
- 10705034214924
- FDA Product Code
- LXH
- EMDN Code
- L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
- GMDN Term
- Orthopaedic implant impactor, reusable
- Device Class
- Class I
- Regulation Number
- 888.4540
- Market of Registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Depuy Spine, Inc.
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No